Admission and mortality data of specific vasculitides
| n | Age | Male | % Died | Age at death | |
|---|---|---|---|---|---|
| Behcets disease | 437 | 36 (29–48) | 36%* | 2% | 63 (42–72) |
| Eosinophilic granulomatosis polyangiitis | 257 | 59 (51–65) | 57%* | 2% | 70 (59–78) |
| Giant cell arteritis | 2187 | 75 (67–81) | 33%* | 3% | 82 (76–86) |
| Goodpasture's syndrome | 432 | 60 (45–73) | 53% | 7% | 70 (60–78) |
| Granulomatosis polyangiitis (GPA) | 1806 | 60 (48–70) | 55%* | 4%* | 72 (63–80) |
| Juvenile polyarteritis | 29 | 10 (8–12) | 3%* | 0% | – |
| Microscopic polyarteritis | 125 | 66 (59–76) | 64%* | 2% | 72 (66–77) |
| Necrotising vasculopathy | 236 | 64 (49–73) | 53% | 7% | 71 55–80) |
| Polyarteritis nodosa | 220 | 51 (39–69) | 52% | 7% | 71 (56–80) |
| Takayasu's arteritis | 112 | 38 (23–54) | 8%* | 0% | – |
Values are whole numbers, percentage and medians (IQR). *Indicates significant gender difference.